Molecule Name DB00199
DrugBank Groups Approved
Cluster No 67
Smiles O=C1(OC(C(O)(C(O)C(C(=O)C(C)CC(C(C(C(C1C)OC2(OC(C(O)C(C2)(OC)C)C))C)OC3(OC(CC(C3O)N(C)C)C))(O)C)C)C)CC)
Download mol2, pdbqt
TPSA 193,91
Non-H Atoms 51
Non-C/H Atoms 14
Metal-Atoms 0
Electronegative Atoms 14
Stereo Centers 18
Rotatable Bonds 7
Rings Closures 3
Small Rings 2
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 47
Symmetric atoms 1
cLogS -3,645
MW 733,933
cLogP 1,6719
HBA 14
HBD 5
Ro5 violations 2
Druglikeness 11,291
DrugScore 0,466073257169356
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Blood-Brain Barrier BBB-
Human Intestinal Absorption HIA+
Caco-2 Permeability Caco2-
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -2,3634
Caco-2 Permeability 2 0,0949
Subcellular localization Lysosome
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor Non-inhibitor
CYP Inhibitory Promiscuity Low CYP Inhibitory Promiscuity
Human Ether-a-go-go-Related Gene Inhibition Weak inhibitor
Human Ether-a-go-go-Related Gene Inhibition 2 Non-inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,4288
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4549
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,2296
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.